Canonical Allele Identifier: CA390746377

Gene: GALC

Linked Data

• MyVariant Identifiers: chr14:g.88414078T>C (hg19) ; chr14:g.87947734T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.87947734T>C , CM000676.2:g.87947734T>C	GRCh38
NC_000014.8:g.88414078T>C , CM000676.1:g.88414078T>C	GRCh37
NC_000014.7:g.87483831T>C	NCBI36
NG_011853.2:g.50830A>G
NG_011853.3:g.50830A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261304.7:c.1483A>G MANE Select	ENSP00000261304.2:p.Asn495Asp
ENST00000261304.6:c.1483A>G	ENSP00000261304.2:p.Asn495Asp
ENST00000393568.8:c.1414A>G	ENSP00000377198.4:p.Asn472Asp
ENST00000393569.6:c.1405A>G	ENSP00000377199.2:p.Asn469Asp
ENST00000544807.6:c.1315A>G	ENSP00000437513.2:p.Asn439Asp
ENST00000555000.5:c.850A>G	ENSP00000450472.1:p.Asn284Asp
ENST00000555179.1:c.200A>G
ENST00000557316.5:c.*881A>G	ENSP00000452314.1:n.*881A>G
NM_000153.3:c.1483A>G	NP_000144.2:p.Asn495Asp
NM_001201401.1:c.1414A>G	NP_001188330.1:p.Asn472Asp
NM_001201402.1:c.1405A>G	NP_001188331.1:p.Asn469Asp
XM_011536618.1:c.1315A>G	XP_011534920.1:p.Asn439Asp
XM_011536618.2:c.1315A>G	XP_011534920.1:p.Asn439Asp
NM_000153.4:c.1483A>G MANE Select	NP_000144.2:p.Asn495Asp
NM_001201401.2:c.1414A>G	NP_001188330.1:p.Asn472Asp
NM_001201402.2:c.1405A>G	NP_001188331.1:p.Asn469Asp